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Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.108620374A>C , CM000685.2:g.108620374A>C
GRCh38
NC_000023.10:g.107863604A>C , CM000685.1:g.107863604A>C
GRCh37
NC_000023.9:g.107750260A>C
NCBI36
NG_011977.1:g.185451A>C
NG_011977.2:g.185451A>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000328300.11:c.2625A>C
MANE Select
ENSP00000331902.7:p.Gly875=
ENST00000361603.7:c.2625A>C
ENSP00000354505.2:p.Gly875=
ENST00000328300.10:c.2625A>C
ENSP00000331902.6:p.Gly875=
ENST00000361603.6:c.2625A>C
ENSP00000354505.2:p.Gly875=
ENST00000483338.1:n.2081A>C
NM_000495.4:c.2625A>C
NP_000486.1:p.Gly875=
NM_033380.2:c.2625A>C
NP_203699.1:p.Gly875=
XM_005262070.2:c.2625A>C
XP_005262127.1:p.Gly875=
XM_005262072.3:c.2625A>C
XP_005262129.1:p.Gly875=
XM_006724616.2:c.2625A>C
XP_006724679.1:p.Gly875=
XM_011530849.1:c.2301A>C
XP_011529151.1:p.Gly767=
XM_011530850.1:c.2625A>C
XP_011529152.1:p.Gly875=
XM_011530851.1:c.198A>C
XP_011529153.1:p.Gly66=
XM_011530849.2:c.2640A>C
XP_011529151.2:p.Gly880=
XM_017029259.2:c.2640A>C
XP_016884748.1:p.Gly880=
XM_017029260.1:c.2640A>C
XP_016884749.1:p.Gly880=
XM_017029261.1:c.2640A>C
XP_016884750.1:p.Gly880=
XM_017029262.2:c.2640A>C
XP_016884751.1:p.Gly880=
XM_017029263.2:c.960A>C
XP_016884752.1:p.Gly320=
NM_000495.5:c.2625A>C
NP_000486.1:p.Gly875=
NM_033380.3:c.2625A>C
MANE Select
NP_203699.1:p.Gly875=